/hypogonadotropic hypogonadism 6 with or without anosmia

hypogonadotropic hypogonadism 6 with or without anosmia

Rare Disease

MONDO:0012988

Also Known As

FGF8 hypogonadotropic hypogonadismhypogonadotropic hypogonadism 6 with or without anosmiahypogonadotropic hypogonadism caused by mutation in FGF8KAL6HH6Kallmann syndrome 6

Definition

Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGF8 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

FGF8 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:612702 ↗

GARD

GARD:10774 ↗

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